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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03473782
Other study ID # 15-00827
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 12, 2015
Est. completion date August 8, 2023

Study information

Verified date August 2023
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a prospective cohort study study with the primary aim of identifying the strongest correlating parameters between voiding diaries and UDS studies most predictive for each type of urologic condition. Investigators will focus on OAB related conditions, as these are symptoms


Recruitment information / eligibility

Status Completed
Enrollment 123
Est. completion date August 8, 2023
Est. primary completion date August 8, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 110 Years
Eligibility Inclusion Criteria: - completing a bladder diary - undergoing VUDS Exclusion Criteria: - have a urinary tract infection - neurogenic bladder - history of pelvic irradiation - prolapse alone without LUTS - pregnant - incarcerated - hospital employee - unable to give consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Voiding Diary
A log kept by each patient to record frequency and volume of urine output and fluid input.
Urodynamics Correlation Study
Provides patho physiological data by assessing bladder sensation, bladder capacity, the presence of involuntary bladder contractions, bladder compliance and bladder outlet obstruction.

Locations

Country Name City State
United States New York University School of Medicine New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure of urgency incontinence using Voiding Diary patients will record urgency in diary 60 Months
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